Autistic People Aren’t Robots

If anything, our feelings are a thousand times more intense than yours.

It’s a strange sensation, discovering that you are part of a minority at the age of 58. This is pure speculation on my part, but if you know something like that all your life, I assume you would not be taken by surprise when people around you spouted ignorant assumptions about who you are. Sure, those prejudices would still be unacceptable and annoying, and even potentially scary, but they wouldn’t shock you. You’d be more prepared for the stupidity by the time you were pushing 60 and had dealt with it all your life.

On the other hand, I feel as though I’m in a frequent state of shock ever since I was diagnosed with Autism Spectrum Disorder back in December. This is an entirely different point of reference for me. I’m learning that, in addition to a drastic alteration in the lens through which I view the world, my diagnosis has also altered the way that people look at me.  

Had I thought things through, perhaps I wouldn’t have disclosed my diagnosis to so many people. But I felt vindicated and relieved at the time. Finally, an explanation! I felt like shouting it from the rooftops. That, and my particular place on the autism spectrum comes with a self-destructive need to overshare.

Whatever. It’s out there. You can’t un-ring a bell.

What really astounds me is that many of these people have known me for years, and yet they’re treating me differently now that I have this label. In a few cases, I could actually see the moment their view of me changed. It is almost as though I’m their eye doctor, and they’re looking at me through that lens machine, and I’m flipping the lenses, and saying, “Better (click), or Worse?”

Worse, apparently.

I came upon a quote recently in an article in Vanity Fair about the rampant toxic racism that was behind the scenes during the filming of the series, “Lost”. I think it applies to my situation as well:

“No one wants to be defined by one aspect of their identity, but neither do people want to feel forced to suppress who they are so that others never feel any discomfort”

Maureen Ryan, in “Lost Illusions: The Untold Story of the Hit Show’s Poisonous Culture

The gut reaction in these situations seems to be to try and “save me” from my diagnosis. “You don’t look autistic!” “That can’t be right. You’ve always seemed normal to me.” “That can’t be right. If anything, you feel too much rather than not enough.” “Why are you making such a big deal out of this?” “I would have never guessed by looking at you.”

Hello! I’m still me! I promise I’m not contagious. And autism is a diagnosis, not a jail sentence. I’m actually coming to think of autism as a “trait”, like blue eyes and brown hair, rather than a “diagnosis”, which implies that I’m sick or flawed and need to be cured. There is no cure for autism, and even if there were, I’m pretty sure I wouldn’t seek it, because it would change the person that I am. I don’t really want someone experimenting with my brain function to that extent.

Of course, that’s easy for me to say, having been able to “pass” as relatively “normal” for decades. Not every autistic person has that luxury. I’m considered to be a level 1 autistc, in other words, I could use some support with my social interactions and my executive function and coping skills, but I’m definitely not a severe autistic.

Level 3 requires very substantial support, often 24 hours a day, and can come with an inability to verbalize and a state of near-constant agitation. Some, but not all people on level three have a low IQ. It would be all but impossible to live independently on that level. Those on that part of the spectrum may appear to be totally unaware of the outside world. But scientists are starting to discover that that may or may not be the case.

I watched a documentary called The Reason I Jump, and now I’m reading the book it was based on. But in the documentary, you meet two non-verbal autistics who learn to spell out their thoughts by pointing to one letter at a time on a chart. And it turns out that they may not speak, but they, in fact, have very intelligent thoughts. No wonder the meltdowns of some non-verbal (along with some verbal) autistics can get violent. Can you imagine being coherent on the inside, but being unable to pierce the chaotic autistic wall that surrounds your brain in order to make your thoughts known to others? That has got to be frustrating beyond belief.

I know what it’s like to be misunderstood. There’s no bigger insult than not being taken seriously. It’s horrible when people constantly seek outside verification before they will believe what you are saying. This has happened to me my entire life, and it hurts.

The worst mistake a neurotypical person can make is to assume that autistic people do not have feelings. If anything, our feelings are a thousand times more intense than yours. It’s like being a full-body burn victim and having people poking you all the time. Our biggest societal challenge, in my opinion, is that many of us have varying degrees of skill at expressing those feelings or properly interpreting the feelings of others.

I understand that Hollywood has done a lot to reinforce the robotic stereotype. Rain Man is only the tip of the cinematic iceberg.

Believe me, we feel. We learn, we grow, and we aren’t going anywhere. So, please be kind.

To quote Shakespeare, “If you prick us, do we not bleed?”

We sure as hell do. But we might be doing so internally. Just because you can’t see it doesn’t mean it doesn’t hurt.

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4 responses to “Autistic People Aren’t Robots”

  1. As you get older, masking gets harder, often trashing social interactions; coping skills are no longer automatic, or easily accessible; and executive functions take a backseat while frustration becomes a constant, unwelcomed companion, as you desperately search for alternatives so you don’t melt down, or Gods forbid, have to ask for inadequate help. I spent my life relying on automatic masking to the point that I didn’t realize I was neurodivergent. It wasn’t till I got older and it became a conscious function to tolerate those things I had successfully pushed into my subconscious, without effort, that I learned I was a closeted level 1 autistc. Wish I’d known earlier so I’d be prepared for this change as I aged. I could have slowly prepared friends and family so they had time to adjust to my changes in those areas. It’s such an energy sucking, bloody chore trying to explain my needs and quirks as they become so visibly real and large. At least the bleeding isn’t hidden anymore and people can’t say they didn’t know. I’m glad you got your diagnosis while you still have the energy and health to deal with the difficulties of getting the support and help we all need to survive in a neurotypical world. Safe journey.

    1. Thank you, my friend. I finally found a therapist who understands neurodivergence, and he’s worth his weight in gold. But I, too, feel the executive functions eroding and the frustration increasing. We autistic adults desperately need more support services.

      1. At least we create our communities and attempt to support each other. We definitely need more from the neurotypical world and it’s professionals. I’m glad they’ve stepped up efforts for children, but we adults, who’ve managed to pass and survive the thousand little cuts endured from navigating the sharp edges of neurotypical environments, don’t appear needy enough, or… they fear us. During my last doctor appointment, her nurse, after overhearing me calmly explain my aversion to touch, treated me like a threat. I’ve no history of violence, or even yelling, during any procedure at any office or clinic, yet she asked another nurse to come help her draw my blood. When asked why she needed back up, she lied and said someone had to push the vial while she held the needle. Really? In one interaction she treated me like a clueless child and a potentially dangerous psych patient. She probably would have preferred me sedated. Fortunately, some physical and occupational therapists have been respectful of my need to avoid overstimlating lights, noise and excessive touching. I still go home exhausted and crawl into bed where sleep offers an escape from the new cuts added to the thousand. Glad you’ve found a good therapist and are proactively expanding your support system. Hang in there.

      2. You too, Lyn. And I know that feeling of suddenly being treated like I’m a bomb that will go off at any minute. Ridiculous.

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